Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,777 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,777 in last 12 months

Showing 4834148360 of 51,768 recalls

Medical DeviceApril 2, 2013· Synvasive Technology Inc

Recalled Item: Product is distributed by Zimmer (Warsaw Recalled by Synvasive Technology...

The Issue: Various reciprocating and oscillating saw blades were incorrectly labeled....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog#...

The Issue: The firm is recalling the specific lot due to lower than expected results.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Fresenius Medical Care Holdings, Inc. dba Renal Solutions

Recalled Item: 2008 MeDS Pump Recalled by Fresenius Medical Care Holdings, Inc. dba Renal...

The Issue: Product is being recalled because the combination of the current 50 mg vial,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14203-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14212-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14210-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14206-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14219-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14217-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14200-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14211-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14207-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Roche Molecular Systems, Inc.

Recalled Item: cobas¿ 4800 system z480 instrument. Integrates fully automated total...

The Issue: In rare instances, channel shifted results have been generated with cobas¿...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 1, 2013· Consumer Concepts, Inc.

Recalled Item: ROCK-IT MAN capsules Recalled by Consumer Concepts, Inc. Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 1, 2013· Lloyd Inc. of Iowa

Recalled Item: Lloyd Thyro-Tab 0.125 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP...

The Issue: cGMP deviations; After quality review of stability failures in previous...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 1, 2013· Lloyd Inc. of Iowa

Recalled Item: Lloyd Thyro-Tab 0.100 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP...

The Issue: cGMP deviations; After quality review of stability failures in previous...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 1, 2013· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: cGMP deviations; After quality review of stability failures in previous...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 1, 2013· Lloyd Inc. of Iowa

Recalled Item: Lloyd Thyro-Tab 0.200 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP...

The Issue: cGMP deviations; After quality review of stability failures in previous...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 1, 2013· Lloyd Inc. of Iowa

Recalled Item: Lloyd Thyro-Tab 0.088 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP...

The Issue: cGMP deviations; After quality review of stability failures in previous...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 1, 2013· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: cGMP deviations; After quality review of stability failures in previous...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund